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重新定义细胞和基因疗法的质量:在学术cGMP设施中实施电子质量管理系统的教训
Xia Wu1, Amaia Cadinanos-Garai1, Vivian Quach1
1USC/CHLA Cell Therapy Program, University of Southern California and Children's Hospital of Los Angeles, Los Angeles, CA 90033, USA.
概括
实施电子质量管理系统 (eQMS) 简化了学术设施中的细胞和基因疗法 (CGT) 制造. 这种过渡提高了效率和监管合规性,克服了资源限制.
科学领域:
- 生物技术是生物技术.
- 制药制造业 制药制造业 制药制造业
- 质量管理系统 质量管理系统
背景情况:
- 细胞和基因疗法 (CGTs) 制造需要严格的质量管理,特别是在资源有限的学术当前良好制造实践 (cGMP) 设置中.
- 传统的基于纸质的质量管理系统 (QMS) 存在诸多挑战,包括错误,可追溯性差,合规风险等.
研究的目的:
- 评估在学术cGMP设施中采用电子质量管理系统 (eQMS) 的好处.
- 为同类机构实施电子质量管理系统提供实用见解和指导.
主要方法:
- 对一个学术cGMP设施 (南加州大学和洛杉矶儿童医院) 的深入案例研究分析.
- 审查实际实施策略,包括平台选择,分阶段推出和员工培训.
主要成果:
- 采用电子质量管理系统导致了运营效率和监管准备度的明显改善.
- 确定了常见的实施挑战,并提出了实际解决方案.
结论:
- 采用eQMS对于学术CGT制造商来说是一个可行的策略,以提高效率和合规性.
- 经验教训为其他机构导航eQMS实施提供了有价值的指导.
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